Incidental Mutation 'IGL02961:Vmn1r184'
ID |
365331 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Vmn1r184
|
Ensembl Gene |
ENSMUSG00000046130 |
Gene Name |
vomeronasal 1 receptor, 184 |
Synonyms |
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.057)
|
Stock # |
IGL02961
|
Quality Score |
|
Status
|
|
Chromosome |
7 |
Chromosomal Location |
25966256-25967200 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 25967075 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Leucine
at position 274
(I274L)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000154576
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000057123]
[ENSMUST00000227230]
[ENSMUST00000227232]
[ENSMUST00000227534]
[ENSMUST00000227790]
[ENSMUST00000228145]
[ENSMUST00000228369]
|
AlphaFold |
E9Q2N4 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000057123
AA Change: I274L
PolyPhen 2
Score 0.274 (Sensitivity: 0.91; Specificity: 0.88)
|
SMART Domains |
Protein: ENSMUSP00000061885 Gene: ENSMUSG00000046130 AA Change: I274L
Domain | Start | End | E-Value | Type |
Pfam:TAS2R
|
8 |
308 |
1.7e-7 |
PFAM |
Pfam:V1R
|
35 |
297 |
7.5e-31 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000227230
AA Change: I274L
PolyPhen 2
Score 0.274 (Sensitivity: 0.91; Specificity: 0.88)
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000227232
AA Change: I274L
PolyPhen 2
Score 0.274 (Sensitivity: 0.91; Specificity: 0.88)
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000227534
AA Change: I274L
PolyPhen 2
Score 0.274 (Sensitivity: 0.91; Specificity: 0.88)
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000227790
AA Change: I274L
PolyPhen 2
Score 0.274 (Sensitivity: 0.91; Specificity: 0.88)
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000228145
AA Change: I274L
PolyPhen 2
Score 0.274 (Sensitivity: 0.91; Specificity: 0.88)
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000228369
AA Change: I274L
PolyPhen 2
Score 0.274 (Sensitivity: 0.91; Specificity: 0.88)
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrv1 |
A |
G |
13: 81,671,731 (GRCm39) |
V2288A |
probably damaging |
Het |
Agbl4 |
T |
A |
4: 110,437,318 (GRCm39) |
N76K |
probably damaging |
Het |
AI182371 |
A |
T |
2: 34,976,124 (GRCm39) |
V258E |
possibly damaging |
Het |
Alg1 |
T |
A |
16: 5,052,861 (GRCm39) |
N80K |
probably benign |
Het |
Ambra1 |
A |
G |
2: 91,741,793 (GRCm39) |
M963V |
possibly damaging |
Het |
Avil |
C |
A |
10: 126,844,175 (GRCm39) |
Q245K |
probably benign |
Het |
Caml |
A |
G |
13: 55,779,695 (GRCm39) |
N256S |
probably benign |
Het |
Ccdc102a |
A |
C |
8: 95,629,978 (GRCm39) |
I521S |
possibly damaging |
Het |
Ccm2l |
A |
G |
2: 152,920,521 (GRCm39) |
T393A |
probably benign |
Het |
Cdh16 |
A |
G |
8: 105,341,837 (GRCm39) |
V91A |
probably damaging |
Het |
Chd7 |
A |
G |
4: 8,751,542 (GRCm39) |
D13G |
probably damaging |
Het |
Chsy1 |
T |
A |
7: 65,821,530 (GRCm39) |
D588E |
probably benign |
Het |
Cilp |
T |
A |
9: 65,185,891 (GRCm39) |
V662E |
possibly damaging |
Het |
Cog8 |
A |
G |
8: 107,782,885 (GRCm39) |
|
probably benign |
Het |
Cpb2 |
T |
C |
14: 75,502,823 (GRCm39) |
V134A |
probably benign |
Het |
Ctcfl |
T |
A |
2: 172,943,712 (GRCm39) |
H546L |
possibly damaging |
Het |
Dclre1c |
A |
G |
2: 3,438,070 (GRCm39) |
D136G |
probably damaging |
Het |
Dnah2 |
T |
A |
11: 69,409,240 (GRCm39) |
E379D |
probably damaging |
Het |
Extl3 |
A |
G |
14: 65,294,408 (GRCm39) |
Y808H |
possibly damaging |
Het |
Gm7247 |
T |
A |
14: 51,602,812 (GRCm39) |
N49K |
probably damaging |
Het |
Insr |
T |
C |
8: 3,308,785 (GRCm39) |
I84V |
probably benign |
Het |
Ipo7 |
C |
T |
7: 109,646,223 (GRCm39) |
P541S |
probably benign |
Het |
Kcnc3 |
T |
C |
7: 44,240,916 (GRCm39) |
S203P |
probably damaging |
Het |
Myo5a |
A |
G |
9: 75,122,402 (GRCm39) |
D1732G |
probably benign |
Het |
Or10q3 |
T |
A |
19: 11,847,695 (GRCm39) |
N295I |
probably damaging |
Het |
Or52d1 |
C |
A |
7: 103,756,357 (GRCm39) |
Y290* |
probably null |
Het |
Or5p68 |
T |
C |
7: 107,945,334 (GRCm39) |
I285V |
probably benign |
Het |
Or5w22 |
A |
G |
2: 87,363,028 (GRCm39) |
Y217C |
probably damaging |
Het |
Or6x1 |
T |
C |
9: 40,098,897 (GRCm39) |
V162A |
probably benign |
Het |
Pde3a |
T |
A |
6: 141,405,426 (GRCm39) |
L426* |
probably null |
Het |
Pkd1 |
T |
A |
17: 24,797,089 (GRCm39) |
D8E |
possibly damaging |
Het |
Polr3a |
A |
T |
14: 24,517,108 (GRCm39) |
Y714* |
probably null |
Het |
Pramel16 |
T |
C |
4: 143,675,717 (GRCm39) |
T370A |
probably damaging |
Het |
Prb1c |
A |
T |
6: 132,338,371 (GRCm39) |
F282L |
unknown |
Het |
Rasgrf1 |
T |
C |
9: 89,863,702 (GRCm39) |
V556A |
possibly damaging |
Het |
Rev3l |
T |
C |
10: 39,703,941 (GRCm39) |
Y1996H |
possibly damaging |
Het |
Rttn |
T |
C |
18: 89,071,697 (GRCm39) |
L1248P |
probably damaging |
Het |
Slc11a1 |
T |
C |
1: 74,416,332 (GRCm39) |
L53P |
probably damaging |
Het |
Slc22a27 |
T |
C |
19: 7,903,886 (GRCm39) |
R84G |
probably damaging |
Het |
Sptbn4 |
A |
G |
7: 27,097,392 (GRCm39) |
L1302P |
probably damaging |
Het |
Srm |
T |
C |
4: 148,678,586 (GRCm39) |
V271A |
possibly damaging |
Het |
Sycp2 |
A |
G |
2: 178,022,655 (GRCm39) |
I492T |
probably benign |
Het |
Tmprss13 |
A |
G |
9: 45,256,301 (GRCm39) |
T472A |
probably damaging |
Het |
Togaram1 |
A |
G |
12: 65,013,484 (GRCm39) |
D245G |
probably damaging |
Het |
Vmn1r21 |
T |
C |
6: 57,820,974 (GRCm39) |
M157V |
probably benign |
Het |
Wdr90 |
C |
A |
17: 26,067,649 (GRCm39) |
E1420* |
probably null |
Het |
Zfp518a |
A |
T |
19: 40,903,462 (GRCm39) |
R1130S |
probably benign |
Het |
|
Other mutations in Vmn1r184 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01396:Vmn1r184
|
APN |
7 |
25,966,862 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01411:Vmn1r184
|
APN |
7 |
25,966,320 (GRCm39) |
missense |
probably benign |
0.06 |
IGL03271:Vmn1r184
|
APN |
7 |
25,967,034 (GRCm39) |
missense |
probably benign |
|
R0302:Vmn1r184
|
UTSW |
7 |
25,966,968 (GRCm39) |
missense |
probably damaging |
1.00 |
R0384:Vmn1r184
|
UTSW |
7 |
25,967,076 (GRCm39) |
missense |
probably benign |
0.41 |
R0591:Vmn1r184
|
UTSW |
7 |
25,966,500 (GRCm39) |
missense |
probably damaging |
0.98 |
R0620:Vmn1r184
|
UTSW |
7 |
25,966,602 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1644:Vmn1r184
|
UTSW |
7 |
25,966,670 (GRCm39) |
missense |
probably benign |
0.00 |
R2304:Vmn1r184
|
UTSW |
7 |
25,966,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R2329:Vmn1r184
|
UTSW |
7 |
25,966,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R3522:Vmn1r184
|
UTSW |
7 |
25,967,008 (GRCm39) |
nonsense |
probably null |
|
R5020:Vmn1r184
|
UTSW |
7 |
25,966,955 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5030:Vmn1r184
|
UTSW |
7 |
25,966,881 (GRCm39) |
missense |
probably benign |
0.25 |
R5049:Vmn1r184
|
UTSW |
7 |
25,966,793 (GRCm39) |
missense |
possibly damaging |
0.49 |
R5076:Vmn1r184
|
UTSW |
7 |
25,966,346 (GRCm39) |
missense |
probably benign |
0.00 |
R5213:Vmn1r184
|
UTSW |
7 |
25,967,136 (GRCm39) |
missense |
probably damaging |
0.99 |
R5554:Vmn1r184
|
UTSW |
7 |
25,966,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R6146:Vmn1r184
|
UTSW |
7 |
25,966,817 (GRCm39) |
missense |
probably benign |
0.08 |
R6868:Vmn1r184
|
UTSW |
7 |
25,966,727 (GRCm39) |
missense |
probably benign |
0.00 |
R6937:Vmn1r184
|
UTSW |
7 |
25,966,750 (GRCm39) |
missense |
probably benign |
0.08 |
R6943:Vmn1r184
|
UTSW |
7 |
25,966,563 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7190:Vmn1r184
|
UTSW |
7 |
25,967,105 (GRCm39) |
missense |
probably damaging |
1.00 |
R7239:Vmn1r184
|
UTSW |
7 |
25,966,602 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7472:Vmn1r184
|
UTSW |
7 |
25,966,824 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8258:Vmn1r184
|
UTSW |
7 |
25,966,686 (GRCm39) |
missense |
probably benign |
0.44 |
R8259:Vmn1r184
|
UTSW |
7 |
25,966,686 (GRCm39) |
missense |
probably benign |
0.44 |
R8911:Vmn1r184
|
UTSW |
7 |
25,966,310 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9008:Vmn1r184
|
UTSW |
7 |
25,967,177 (GRCm39) |
missense |
probably benign |
|
R9159:Vmn1r184
|
UTSW |
7 |
25,966,545 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9216:Vmn1r184
|
UTSW |
7 |
25,966,703 (GRCm39) |
missense |
probably benign |
0.00 |
R9548:Vmn1r184
|
UTSW |
7 |
25,966,734 (GRCm39) |
missense |
probably benign |
0.29 |
R9588:Vmn1r184
|
UTSW |
7 |
25,966,347 (GRCm39) |
missense |
probably null |
0.78 |
Z1177:Vmn1r184
|
UTSW |
7 |
25,966,415 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
Posted On |
2015-12-18 |